首页> 外文期刊>Journal of Radiation Research: Official Organ of the Japan Radiation Research Society >Chemical repair activity of free radical scavenger edaravone: reduction reactions with dGMP hydroxyl radical adducts and suppression of base lesions and AP sites on irradiated plasmid DNA
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Chemical repair activity of free radical scavenger edaravone: reduction reactions with dGMP hydroxyl radical adducts and suppression of base lesions and AP sites on irradiated plasmid DNA

机译:自由基清除剂依达拉奉的化学修复活性:与dGMP羟基自由基加合物的还原反应以及对辐射质粒DNA上碱基损伤和AP位点的抑制

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摘要

Reactions of edaravone (3-methyl-1-phenyl-2-pyrazolin-5-one) with deoxyguanosine monophosphate (dGMP) hydroxyl radical adducts were investigated by pulse radiolysis technique. Edaravone was found to reduce the dGMP hydroxyl radical adducts through electron transfer reactions. The rate constants of the reactions were greater than 4 x 10(8) dm(3) mol(-1) s(-1) and similar to those of the reactions of ascorbic acid, which is a representative antioxidant. Yields of single-strand breaks, base lesions, and abasic sites produced in pUC18 plasmid DNA by gamma ray irradiation in the presence of low concentrations (10-1000 mu mol dm(-3)) of edaravone were also quantified, and the chemical repair activity of edaravone was estimated by a method recently developed by the authors. By comparing suppression efficiencies to the induction of each DNA lesion, it was found that base lesions and abasic sites were suppressed by the chemical repair activity of edaravone, although the suppression of single-strand breaks was not very effective. This phenomenon was attributed to the chemical repair activity of edaravone toward base lesions and abasic sites. However, the chemical repair activity of edaravone for base lesions was lower than that of ascorbic acid.
机译:通过脉冲辐射分析技术研究了依达拉奉(3-甲基-1-苯基-2-吡唑啉-5-酮)与单氧脱氧鸟苷(dGMP)羟基自由基加合物的反应。发现依达拉奉可通过电子转移反应还原dG​​MP羟基自由基加合物。反应的速率常数大于4 x 10(8)dm(3)mol(-1)s(-1),与抗氧化剂抗坏血酸的反应速率常数相似。在低浓度(10-1000μmol dm(-3))依达拉奉的存在下,γ射线辐照在pUC18质粒DNA中产生的单链断裂,碱基损伤和无碱基位点的产量也被定量,并且化学修复作者最近开发了一种方法来评估依达拉奉的活性。通过比较抑制效率与每个DNA损伤的诱导,发现依达拉奉的化学修复活性可以抑制基础损伤和无碱基位点,尽管单链断裂的抑制作用不是很有效。这种现象归因于依达拉奉对基础病变和无基础位点的化学修复活性。然而,依达拉奉对基础病变的化学修复活性低于抗坏血酸。

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